SANDOZ FINGOLIMOD CAPSULE

Država: Kanada

Jezik: angleščina

Source: Health Canada

Aktivna sestavina:

FINGOLIMOD (FINGOLIMOD HYDROCHLORIDE)

Dostopno od:

SANDOZ CANADA INCORPORATED

Koda artikla:

L04AE01

INN (mednarodno ime):

FINGOLIMOD

Odmerek:

0.5MG

Farmacevtska oblika:

CAPSULE

Sestava:

FINGOLIMOD (FINGOLIMOD HYDROCHLORIDE) 0.5MG

Pot uporabe:

ORAL

Enote v paketu:

28

Tip zastaranja:

Prescription

Terapevtsko območje:

Immunomodulatory Agents

Povzetek izdelek:

Active ingredient group (AIG) number: 0152886001; AHFS:

Status dovoljenje:

APPROVED

Datum dovoljenje:

2019-03-11

Lastnosti izdelka

_Sandoz Fingolimod _
_Page 1 of 68 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
SANDOZ
® FINGOLIMOD
Fingolimod capsules
Capsule, 0.5 mg fingolimod (as fingolimod hydrochloride), Oral
Sphingosine 1-phosphate receptor modulator
Sandoz Canada Inc.
110, Rue de Lauzon
Boucherville, Québec, Canada
J4B 1E6
Date of Inital Authorization:
October 31, 2019
Date of Revision:
February 23, 2022
Submission Control No: 256559
_Sandoz Fingolimod _
_Page 2 of 68 _
RECENT MAJOR LABEL CHANGES
2 Contraindications
02/2022
4 Dosage and administration
02/2022
7 Warnings and Precautions
02/2022
TABLE OF CONTENTS
RECENT MAJOR LABEL
CHANGES..............................................................................................2
TABLE OF CONTENTS
................................................................................................................2
PART I: HEALTH PROFESSIONAL INFORMATION
.......................................................................4
1
INDICATIONS
................................................................................................................4
1.1
PEDIATRICS
............................................................................................................4
1.2
GERIATRICS
............................................................................................................4
2
CONTRAINDICATIONS ..................................................................................................
4
4
DOSAGE AND ADMINISTRATION
..................................................................................
5
4.1
DOSING
CONSIDERATIONS.........................................................................................5
4.2
RECOMMENDED DOSE AND DOSAGE ADJUSTMENT
.....................................................7
4.4
ADMINISTRATION
....................................................................................................8
4.5
MISSED
DOSE.......................................................................................................